Evidence map›Paper›PMID 24650451›Full record

ArticlePsychiatry research2014

The relationship between fasting serum glucose and cerebral glucose metabolism in late-life depression and normal aging.

Christopher M Marano, Clifford I Workman, Christopher H Lyman, Elisse Kramer, Carol R Hermann, Yilong Ma, Vijay Dhawan, Thomas Chaly, David Eidelberg, Gwenn S Smith

Abstract read
In one paragraph

Article in Psychiatry research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Pooled it
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  8. Review
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  10. Hemoglobin ADiabetes care · 2017
    Observational
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 1 country.

Christopher M MaranoDepartment of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, MD 21224, USA.
Clifford I WorkmanDepartment of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, MD 21224, USA.
Christopher H LymanDepartment of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, MD 21224, USA.
Elisse KramerDepartment of Geriatric Psychiatry, The Zucker Hillside Hospital, Glen Oaks, NY 11004, USA.
Carol R HermannDepartment of Geriatric Psychiatry, The Zucker Hillside Hospital, Glen Oaks, NY 11004, USA.
Yilong MaCenter for Neurosciences, The Feinstein Institute for Medical Research, North Shore - Long Island Jewish Health System, Manhasset, NY 11030, USA.
Vijay DhawanCenter for Neurosciences, The Feinstein Institute for Medical Research, North Shore - Long Island Jewish Health System, Manhasset, NY 11030, USA.
Thomas ChalyCenter for Neurosciences, The Feinstein Institute for Medical Research, North Shore - Long Island Jewish Health System, Manhasset, NY 11030, USA.
David EidelbergCenter for Neurosciences, The Feinstein Institute for Medical Research, North Shore - Long Island Jewish Health System, Manhasset, NY 11030, USA.
Gwenn S SmithDepartment of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, MD 21224, USA. Electronic address: gsmith95@jhmi.edu.
Feinstein Institute for Medical Research · USJohns Hopkins University · USZucker Hillside Hospital · USJohns Hopkins Medicine · US

Funding

'T V ASSESSMENT - MEMORY DISORDERED PATIENTS'P50AG005146 · NIA · JOHNS HOPKINS UNIVERSITY · PI TRONCOSO, JUAN · 1985 to 2019
$37.6M
WHITE MATTER STRUCTURAL DEFICITS IN HIGH FUNCTIONING CHILDREN WITH AUTISM SPEM01RR018535 · NCRR · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI MATTIS, PAUL · 2003 to 2010
$19.5M
Serotonin Modulation in Geriatric DepressionR01MH064823 · NIMH · JOHNS HOPKINS UNIVERSITY · PI SMITH, GWENN S. · 2003 to 2006
$1.9M
Insulin Resistance in Late-Life DepressionK23MH095971 · NIMH · JOHNS HOPKINS UNIVERSITY · PI MARANO, CHRISTOPHER · 2012 to 2016
$903k
MONOAMINERGIC FUNCTION IN GERIATRIC NEUROPSYCHIATRYK02MH001621 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SMITH, GWENN S · 1998 to 2008
$884k
PET STUDIES OF CHOLINERGIC MODULATION IN ALZHEIMERSR01MH057078 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SMITH, GWENN S · 1997 to 2000
$293k
PET STUDIES OF NEUROTRANSMITTER INTERACTIONS IN HUMANSR01MH049936 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SMITH, GWENN S · 1993 to 1999
–
NCRR NIH HHS M01 RR018535NCRR NIH HHS M01RR018535NIA NIH HHS P50 AG005146NIMH NIH HHS K02 MH001621NIMH NIH HHS K23 MH095971NIMH NIH HHS MH49936NIMH NIH HHS MH57078NIMH NIH HHS MH64823NIMH NIH HHS R01 MH057078NIMH NIH HHS R01 MH064823
6 · The paper itself

Abstract

Evidence exists for late-life depression (LLD) as both a prodrome of and risk factor for Alzheimer׳s disease (AD). The underlying neurobiological mechanisms are poorly understood. Impaired peripheral glucose metabolism may explain the association between depression and AD given the connection between type 2 diabetes mellitus with both depression and AD. Positron emission tomography (PET) measures of cerebral glucose metabolism are sensitive to detecting changes in neural circuitry in LLD and AD. Fasting serum glucose (FSG) in non-diabetic young (YC; n=20) and elderly controls (EC; n=12) and LLD patients (n=16) was correlated with PET scans of cerebral glucose metabolism on a voxel-wise basis. The negative correlations were more extensive in EC versus YC and in LLD patients versus EC. Increased FSG correlated with decreased cerebral glucose metabolism in LLD patients to a greater extent than in EC in heteromodal association cortices involved in mood symptoms and cognitive deficits observed in LLD and dementia. Negative correlations in YC were observed in sensory and motor regions. Understanding the neurobiological consequences of diabetes and associated conditions will have substantial public health significance given that this is a modifiable risk factor for which prevention strategies could have an important impact on lowering dementia risk.

Indexed as

AdultAgedAgingBlood GlucoseCerebral CortexDepressive DisorderFastingFemaleGlucoseHumansMaleMiddle AgedPositron-Emission TomographyYoung AdultBlood GlucoseGlucoseFasting blood glucoseFDG PETInsulin resistanceLate-life depressionNormal aging

Identifiers

PMID24650451
PMCPMC4388739
OpenAlexW2068156124

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.